Chemist Jobs in Ballwin, MO

BYK Additives & Instruments is one of the world's leading suppliers in the field of additives and measuring instruments. Around the world, the additives of BYK ensure that coatings and plastics precisely obtain the desired properties and the correct quality. We're looking for a highly motivated, experienced Senior Chemist to join our production team! Excellent Medical, Dental, and Vision Benefit plans eligible to enroll within 30 days of hire Annual Merit increases, Bonuses, and 401K Discretionary company match up to 5%! Opportunity for advancement and training opportunities for all employees. SUMMARY: The ADP Sr. Chemist will primarily be responsible for new product development that addresses the needs of different thermoplastic end-use applications, e.g. automotive, industrial, etc. This role will report to the head of ADP and work to provide technical leadership and direction to the ADP team. DUTIES: New product development through the design and development novel plastic additive formulations Design experiments to evaluate performance of additive formulations using plastics processing and testing equipment and reporting data from such studies Perform testing on competitive products, commercial products, and plastics samples as needed work directly with manufacturing to address production issues and process optimization Author technical reports for internal and external customers Perform plastic processing, compounding and plastics forming Responsible for shipping high-quality customer samples in a timely manner, in accordance with domestic and international regulations The successful candidate will write work instructions and Standard Operating Procedures. The successful candidate will interface with operations to translate successful lab-scale projects to production. Maintain laboratory equipment Responsible for working with, handling, shipping, ordering, and storing chemicals in a safe and environmentally responsible manner as outlined in Safety Data Sheets, and in accordance with company and governmental regulations Special assignments, projects, and process improvement initiatives; as assigned by ADP management Will be responsible for managing direct reports QUALIFICATIONS: Working knowledge relating to chemical processes, plastic applications or laboratory applications Understand safety implications with respect to equipment, processes, and chemicals in the laboratory and manufacturing environments Highly skilled in the use of computer programs necessary for data entry and data analysis (e.g. Microsoft Word, PowerPoint, Excel, etc.) Good verbal and written communication skills Ability to drive self-directed projects to completion in a team-oriented collaborative work environment Able to lift 50 pounds. Able to travel both domestically and internationally Working knowledge of formulation ingredients and the processing of thermoplastics or thermosets is preferred EDUCATION AND EXPERIENCE: PhD Preferred, Master's Required Practical experience in a lab or production setting is necessary. Ideally, two years of experience in industrial manufacturing and knowledge of the plastics industry. Experience with analytical lab testing, data analysis and presentations are required Experience with plastic processing technologies (extrusion, molding and testing) is preferred. Experience working with mechanical equipment is preferred. This role is not eligible for sponsorship. In the ALTANA Group, you will work in a unique culture of innovation where the utmost importance is attached to promoting individual ideas and abilities as well as open, trusting interaction. ALTANA AG and its subsidiaries is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

divstrong Description/strongbr/pspan Want to join a world leader? Then Sensient may be for you! At Sensient Technologies, we are experts in science, art, and innovation of color and flavor. We are market savvy and visionary. We are problem solvers and we will be better with you. /span/p pspan As the bProcess Chemist Manager/b, you will l/spanspanead a team of four (4)/spanspan in the optimization and standardization of new and existing manufacturing processes to achieve maximum quality and yield at the lowest manufacturing costs through in-depth process studies and implementation of best practices. You will support key product profitability goals through successful introduction of new Ramp;D scale process to the plant floor. /spanspan /span/p pb What You'll Do: /b/p ul li Manager the continuous optimization of our processes in order to achieve the lowest manufacturing cost while maintaining high quality. Continuously monitor yield and raw material usage of target, take action on issues that arise. /li li Report on performance yield vs std yield. Collaborate with cross functional teams./li li Assist operations and quality in trouble shooting process problems. Identify and help implement permanent solutions to chronic exceptions./li li Serve as manufacturing Representative on new product / process introductions into the manufacturing plant./li li Function as liaison between production and Ramp;D. Drive accountability with our process chemists / operational excellence team. Lead or serve as a key member on assigned quality Improvement Teams./li li Maintain a trained staff and embrace our coaching and continual improvement approach. Assist in development and maintenance of standard Operation Procedures, Job Models and Exception Condition reports. /li /ul pb What You'll Bring: /b/p ul liM.S. or PhD Degree in Chemistry with a minimum of 10 years of industry experience. /li li Experience with synthetic reactions, rheology and organic chemistry. /li li Previous operations management experience is a plus. Proven troubleshooting record with emphasis in root cause analysis and cost/benefit evaluation. /li li Willingness to provide hands on support to troubleshoot and commission processes. /li li Food / Pharmaceutical or other FDA regulated industry experience is a plus./li /ul pspanb What You'll Get: /b/span/p ul li Opportunity to collaborate with your colleagues, onsite 5-days per week./li li An excellent salary, benefit offering, and development opportunities./li liA thorough and effective training experience during onboarding and beyond. /li /ul p style="margin-left:.25in"spanb SPONSORSHIP: Due to our inability to offer visa sponsorship, we can only consider candidates who are authorized to work in the United States without the need for employment visa sponsorship. /b/span/p p style="margin-left:.25in"span About Sensient: Sensient Technologies Corporation is a leading global manufacturer and marketer of colors, flavors, and extracts. Sensient employs advanced technologies at facilities around the world to develop specialty food and beverage systems, cosmetic and pharmaceutical systems, specialty colors, and other specialty and fine chemicals. The Company's customers include major international manufacturers representing most of the world's best-known brands. /span/p p style="margin-left:.25in"span About Sensient Colors: Sensient Colors is a leading developer, producer, and supplier of natural and synthetic color systems for customers around the globe. The Company's high-performance products play a vital role in the manufacture of foods and beverages, cosmetic and pharmaceutical/span/p p style="margin-left:.25in"span Equal Opportunity Employer/span/p p style="margin-left:.25in"span#LI-BW1/span/pbr/br//div

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description We are seeking a highly skilled and motivated Chemist II to join our dynamic team in St. Louis. The ideal candidate will have 2-5 years of industry experience and a strong background in analytical instrumentation, preferably with Inductively Coupled Plasma Mass Spectrometry (ICPMS) and/or Gas Chromatography with Mass Spectrometry (GCMS) experience. This role offers an exciting opportunity to contribute to cutting-edge research and development projects within our organization. Key Responsibilities: Perform routine and complex analyses using ICPMS, GCMS and/or other analytical instrumentation (HPLC, LCMS, etc.) to support various research and development projects. Develop and validate analytical methods for the detection and quantification of trace elements and other compounds. Interpret and report analytical data, ensuring accuracy and compliance with industry standards. Collaborate with cross-functional teams to support project goals and timelines. Maintain and troubleshoot laboratory equipment, ensuring optimal performance. Document experimental procedures and results in accordance with company protocols. Qualifications Bachelor's or Master's degree in Chemistry or a related field. 2-5 years of industry experience, with a focus on ICPMS and/or GCMS preferred. Strong analytical and problem-solving skills. Excellent attention to detail and ability to work independently. Effective communication and teamwork skills. Familiarity with laboratory safety protocols and best practices. Preferred Qualifications: Experience with method development and validation. Experience following established methods and/or protocols. Knowledge of regulatory requirements and quality control procedures. Proficiency in Microsoft products (word, excel, etc.). Additional Information Position is a full time Monday-Friday, 8-5 p.m., with overtime as needed. Candidates within commutable distance to St. Louis, MO are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA BioPharma Services is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Industrial Inspection & Analysis is looking to hire a Chemist at our materials testing laboratory located in St. Louis, MO. IIA's Lab Services has grown to be one of the largest dedicated quality service providers in the nation. We work across a spectrum of industries to solve quality challenges and help companies grow with capacity and capability. We strive for story-worthy customer service. Primary Job Responsibilities The primary job function is to perform chemical compositional analyses of numerous materials from various industries utilizing instrumentation including but not limited to ICP-MS, ICP-OES, SEM/EDS, and XRF. The Chemist will also: Prepare reagents, prep samples consisting of complex matrixes (products), liquids, and solid materials and analyze according to published methods. Work effectively, under minimum direction, in a team environment delivering test results in sample hold time and on time. Perform acid digestion of various metals, ores, and slags materials to identify the chemical composition and best match to industry standard Create beneficial customer relationship through accurate and timely communication Maintenance of equipment, routine, and non-routine. Required Qualifications Must be a U.S. Citizen or Permanent Resident Bachelor's Degree in Chemistry Minimum 3-5 years of experience in ICP-MS and/or ICP-OES Excellent mathematical skills Detail oriented A self-directed mindset with the ability to work under minimal supervision is critical to this position Able to effectively communicate questions and differences between common problems and unique situations Ability to organize work and to engage in a variety of tasks simultaneously and consistently to meet deadlines is essential to this position Familiar with Microsoft Excel and Microsoft Word Work well in group solving situations Working Conditions Work will be performed primarily in lab and occasionally onsite at client facility Must be able to stand for long periods of time while performing the job responsibilities. Must be able to regularly lift and/or move up to 25 pounds. Benefits Offered Medical, Dental, Vision 401K Paid Time Off and Holidays Life Insurance Disability

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description We are seeking a highly skilled and motivated Chemist II to join our dynamic team in St. Louis. The ideal candidate will have 2-5 years of industry experience and a strong background in analytical instrumentation, preferably with Inductively Coupled Plasma Mass Spectrometry (ICPMS) and/or Gas Chromatography with Mass Spectrometry (GCMS) experience. This role offers an exciting opportunity to contribute to cutting-edge research and development projects within our organization. Key Responsibilities: * Perform routine and complex analyses using ICPMS, GCMS and/or other analytical instrumentation (HPLC, LCMS, etc.) to support various research and development projects. * Develop and validate analytical methods for the detection and quantification of trace elements and other compounds. * Interpret and report analytical data, ensuring accuracy and compliance with industry standards. * Collaborate with cross-functional teams to support project goals and timelines. * Maintain and troubleshoot laboratory equipment, ensuring optimal performance. * Document experimental procedures and results in accordance with company protocols. Qualifications * Bachelor's or Master's degree in Chemistry or a related field. * 2-5 years of industry experience, with a focus on ICPMS and/or GCMS preferred. * Strong analytical and problem-solving skills. * Excellent attention to detail and ability to work independently. * Effective communication and teamwork skills. * Familiarity with laboratory safety protocols and best practices. Preferred Qualifications: * Experience with method development and validation. * Experience following established methods and/or protocols. * Knowledge of regulatory requirements and quality control procedures. * Proficiency in Microsoft products (word, excel, etc.). Additional Information Position is a full time Monday-Friday, 8-5 p.m., with overtime as needed. Candidates within commutable distance to St. Louis, MO are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA BioPharma Services is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make In this role, you will be responsible for accurately recording and reporting data in full compliance with current methods, Standard Operating Procedures (SOPs), United States Pharmacopeia (USP/NF), relevant compendia, and cGMP regulations. You will leverage your expertise in high-performance liquid chromatography (HPLC), gas chromatography (GC), Chromatography Data Software applications, titrations, pH measurement, Karl Fischer analysis, and general wet chemistry/compendial testing to ensure precise and reliable analytical results. Your attention to detail and commitment to regulatory excellence will be critical in maintaining quality and compliance within the laboratory environment. Role Responsibilities o Performs/coordinates routine set up, calibration, operation, and maintenance of laboratory test instruments/equipment as needed. o Analyzes samples using various techniques/instrumentation per established departmental/site/corporate policies/compendial pharmacopoeia specifications, and procedures. o Prepares solutions and standardizes test solutions as defined in analytical method or compendia. o Practices cGMP, which includes, but is not limited to, proper laboratory documentation and maintenance, archival of documentation/raw data, peer review, attention to specification limits for any tests performed, and immediate notification of any out-of-specification (OOS) results. o Compiles reports/documentation of analytical tests, ensuring reports are accurate and complete with documentation of procedures, equipment/instruments, and reagents used in analytical testing. o Reviews and revises SOPs, analytical methods and related procedures/documents. May recommend clarification or request optimization of test methods/procedures for consistent/compliant processes. o Lead/coordinate training of colleagues for qualification on additional test methods/procedures. Basic Qualifications Knowledge of compendia; USP, EP, and others as applicable, cGMP guidelines, FDA regulations; laboratory safety procedures, laboratory instrumentation, and SDS; knowledge of inorganic and organic chemistry principals.

Driven by integrity and united by the people-and-pet bond, we find strong purpose in the work we do and an even greater joy in those we get to work alongside. Together, we harness the expertise of our long-standing tradition of excellence to embrace possibility and continuously push to do what's never been done before in pet care. Discover your purpose and fuel your passions when you bring your love of pets to a team that prides itself on the power of togetherness-We are Proudly Connected. Purely Driven. Position Summary Quality Assurance and Nestlé Purina Analytical Laboratories department is comprised of talented individuals who possess a genuine love for pets and their families. We thrive on being at the forefront of research, contributing to the innovation and advancements in pet nutrition and quality that sets Nestlé Purina apart. Ensuring the delivery of safe ingredients and sustainable practices to our factories and beyond, we are invigorated by the extensive research and development that goes into our products. Bring your impact to the table and together we will continue to work towards being one of the most trusted companies in pet care. As an Analytical Chemist, you will execute and interpret complex procedures and protocols within a project or goal. You'll be a great fit if you are a self-starter who takes initiative and works independently while collaborating within Nestlé Purina Analytics Laboratories (NPAL). You'll be expected to learn method development, make process improvements, and help draft standard operating procedures (SOP's) in addition to mentoring other team members. * Prepare and interpret reports of complex experiments * Follow established methods and procedures to deliver timely results * Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals * Assist in development and validation of analytical methods in support of projects * Aid in experiments and project assignments Requirements * Bachelor's degree in Chemistry or a related field * 3+ years of analytical lab or industry experience, analytical instrumentation experience, and troubleshooting of assay and equipment issues * 2+ years of experience with chromatography and/or mass spectrometry (HPLC, GC, GCMS, LCMS, etc.) Other * 1+ years of experience working in an ISO 17025 accredited laboratory is preferred * Must be willing to work Tuesday through Saturday from 8:00AM to 5:00PM Environment includes exposure to Top 14 Allergens. The approximate pay range for this position is $59,000.00 to $90,000.00. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities as well as geographic location of the position. Nestlé offers performance-based incentives and a competitive total rewards package, which includes a 401k with Company match, healthcare coverage and a broad range of other benefits. Incentives and/or benefit packages may vary depending on the position. Learn more at About Us | Making an Impact | Nestle Careers (nestlejobs.com). REQUISITION ID 345728 It is our business imperative to remain a very inclusive workplace. To our veterans and separated service members, you're at the forefront of our minds as we recruit top talent to join Nestlé. The skills you've gained while serving our country, such as flexibility, agility, and leadership, are much like the skills that will make you successful in this role. In addition, with our commitment to an inclusive work environment, we recognize the exceptional engagement and innovation displayed by individuals with disabilities. Nestlé seeks such skilled and qualified individuals to share our mission where you'll join a cohort of others who have chosen to call Nestlé home. The Nestlé Companies are equal employment opportunity employers. All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status or any other characteristic protected by applicable law. Prior to the next step in the recruiting process, we welcome you to inform us confidentially if you may require any special accommodations in order to participate fully in our recruitment experience. Contact us at accommodations@nestle.com or please dial 711 and provide this number to the operator: **************. This position is not eligible for Visa Sponsorship. Review our applicant privacy notice before applying at *********************************** Driven by integrity and united by the people-and-pet bond, we find strong purpose in the work we do and an even greater joy in those we get to work alongside. Together, we harness the expertise of our long-standing tradition of excellence to embrace possibility and continuously push to do what's never been done before in pet care. Discover your purpose and fuel your passions when you bring your love of pets to a team that prides itself on the power of togetherness-We are Proudly Connected. Purely Driven. Position Summary Quality Assurance and Nestlé Purina Analytical Laboratories department is comprised of talented individuals who possess a genuine love for pets and their families. We thrive on being at the forefront of research, contributing to the innovation and advancements in pet nutrition and quality that sets Nestlé Purina apart. Ensuring the delivery of safe ingredients and sustainable practices to our factories and beyond, we are invigorated by the extensive research and development that goes into our products. Bring your impact to the table and together we will continue to work towards being one of the most trusted companies in pet care. As an Analytical Chemist, you will execute and interpret complex procedures and protocols within a project or goal. You'll be a great fit if you are a self-starter who takes initiative and works independently while collaborating within Nestlé Purina Analytics Laboratories (NPAL). You'll be expected to learn method development, make process improvements, and help draft standard operating procedures (SOP's) in addition to mentoring other team members. * Prepare and interpret reports of complex experiments * Follow established methods and procedures to deliver timely results * Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals * Assist in development and validation of analytical methods in support of projects * Aid in experiments and project assignments Requirements * Bachelor's degree in Chemistry or a related field * 3+ years of analytical lab or industry experience, analytical instrumentation experience, and troubleshooting of assay and equipment issues * 2+ years of experience with chromatography and/or mass spectrometry (HPLC, GC, GCMS, LCMS, etc.) Other * 1+ years of experience working in an ISO 17025 accredited laboratory is preferred * Must be willing to work Tuesday through Saturday from 8:00AM to 5:00PM Environment includes exposure to Top 14 Allergens. The approximate pay range for this position is $59,000.00 to $90,000.00. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities as well as geographic location of the position. Nestlé offers performance-based incentives and a competitive total rewards package, which includes a 401k with Company match, healthcare coverage and a broad range of other benefits. Incentives and/or benefit packages may vary depending on the position. Learn more at About Us | Making an Impact | Nestle Careers (nestlejobs.com). REQUISITION ID 345728 It is our business imperative to remain a very inclusive workplace. To our veterans and separated service members, you're at the forefront of our minds as we recruit top talent to join Nestlé. The skills you've gained while serving our country, such as flexibility, agility, and leadership, are much like the skills that will make you successful in this role. In addition, with our commitment to an inclusive work environment, we recognize the exceptional engagement and innovation displayed by individuals with disabilities. Nestlé seeks such skilled and qualified individuals to share our mission where you'll join a cohort of others who have chosen to call Nestlé home. The Nestlé Companies are equal employment opportunity employers. All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status or any other characteristic protected by applicable law. Prior to the next step in the recruiting process, we welcome you to inform us confidentially if you may require any special accommodations in order to participate fully in our recruitment experience. Contact us at accommodations@nestle.com or please dial 711 and provide this number to the operator: **************. This position is not eligible for Visa Sponsorship. Review our applicant privacy notice before applying at *********************************** St. Louis, MO, US, 63102 St. Louis, MO, US, 63102

We are seeking a skilled Analytical Chemist to support late-stage development and lifecycle management within our Global Technical Operations team. In this dynamic role, you will leverage your expertise in analytical method development, validation, and transfer to both internal and external GMP laboratories. You will play a critical role in the isolation and characterization of trace-level impurities in drug substances and drug products, ensuring the highest standards of data quality and regulatory compliance. This position offers the opportunity to collaborate in a cross-functional environment, working closely with teams in Process Chemistry, Formulation, Quality, Operations, and Regulatory to drive the successful execution of key deliverables. Essential Functions Lead project planning by defining functions, setting timelines, coordinating resources, and ensuring on-time execution. Develop innovative solutions for complex challenges using critical thinking, creativity, and collaboration while considering downstream impacts. Maintain accurate and detailed records in laboratory notebooks and uphold the highest safety standards. Prepare regulatory documentation to support filings and compliance requirements. Provide strategic input to resolve analytical chemistry challenges within Global Technical Operations. Collaborate cross-functionally in a matrix environment to drive project success. Contribute to scientific advancements through new technologies, publications, patents, or trade secrets. Minimum Requirements BA or BS in Analytical Chemistry or related science typically with a minimum of 5 years of pharmaceutical/biotech or related work experience in industry. MS in Analytical Chemistry or related science typically with a minimum of 2 years of pharmaceutical/biotech or related work experience in industry. PhD in Analytical Chemistry or related science Extensive hands-on experience with HPLC/UPLC, LC-MS, GC, GC-MS, TGA, DSC, UV, and IR spectroscopy for drug characterization and quantitation. Expertise in method development, validation, and transfer for small molecules, peptides, and biologics. Strong analytical chemistry problem-solving skills, including trace-level impurity characterization in drug substances and products. Experience with extractable and leachable analysis, biocompatibility testing, and chemical characterization. Knowledge of regulatory standards, including ISO 10993, ISO 18562, EU MDR (GSPR), ICH guidelines, and pharmacopeial requirements. Familiarity with QbD method development tools and regulatory compliance. Self-starter with a strong work ethic, communication, and project management skills. Ability to work independently and collaboratively in a cross-functional team environment. Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Project, Visio) and Adobe. Strong organizational, planning, and interpersonal skills. Preferred Skills Strong familiarity with pharmaceutical GMP and regulatory guidelines Practical experience in bioanalytical chemistry Experience with administration and/or support of Waters Empower Experience with Agilent and Waters analytical instruments and associated software Organizational Relationship/Scope: Position directly reports to the Sr. Manager, Analytical Chemistry. Working Conditions: This position requires frequent work in a research laboratory, both standing at a bench and seated. It also requires reaching into flammable cabinets. This position involves frequent work in an office environment, using a computer to analyze data and write reports and documenting experiments in notebooks. Occasional travel may be required for engagement with external laboratories and collaborators. #LI-LM1

Experiencing together a unique human adventure Animal health is key to the health of the planet. Working at Virbac means taking part in a unique human adventure in which the engagement of each individual contributes to its evolution. Encouraging internal mobility between positions and countries, offering individual development plans and building a partnership based on trust between managers and employees are as many perspectives of motivation for our teams. We also offer them a work environment conducive to exploring new territories and balancing their professional and personal lives. Finally, fostering their engagement to animal health also means listening to them and helping them to acquire new skills, preparing them for the challenges of tomorrow and encouraging them to contribute to an ever more responsible approach to our business. R&D Analytical Development Chemist Virbac Animal Health is seeking an Analytical Development Chemist III to join our team. The Analytical Development Chemist III independently develops analytical methodology, validation, and transfer projects for existing and development products for the performance of routine analytical testing on finished products and stability samples. Design and execute studies to demonstrate the validity of test methods. Perform routine and non-routine testing as required to support R&D. Plan, manage and execute analytical projects within a cGMO environment, and prescribed timelines and budget. Qualified candidates must possess, at a minimum, a BS in Chemistry or equivalent science degrees 5 to 10 years of experience. 5+ years of prior experience working in an analytical test lab with experience in developing and validating methods in cGMP environment. This exciting position will work in Bridgeton, MO. It comes with an excellent benefits package including generous time off, 401k + match, life, medical, dental, and vision benefits, and more! Responsabilities Area of responsibility 1: [Exhibit expert skills in method development for evaluating the product characteristics, assay, dissolution and related substances through independent research] Main activities * Perform complex analysis using unfamiliar or new methods Expected results: Methods suitable for supporting product registration Area of responsibility 2: [Actively demonstrate expert level knowledge of a wide range of analytical techniques, methods, chemical principles, and laboratory practices] Main activities * Use deep technical knowledge to develop new applications of technologies Expected results: Accurate and reliable testing methods for development products. Area of responsibility 3 : [Successfully plan, manage and execute analytical projects within prescribed timelines and budgets] Main activities Quantify performance and project results * Manage your own time to ensure you complete project planning and execution tasks on time, and schedule * and manage Analytical Chemist I and II priorities and time * * Ability to convey ideas and information in ways others can understand. Project management requires this * skill for both written and verbal communication with individuals and groups Expected results: Completion of analytical project objectives and schedule Area of responsibility 4: [Highly self-motivated, team oriented individual that can work independently without supervision]. Main activities * Demonstrates a deep knowledge of a wide range of analytical techniques, read and interpret USP and other guidance documents * * Perform critical interpretations of data, suggest solutions for problems, execute those solutions and report results * Expected results: Work without daily instruction from supervisor for work demands Area of responsibility 5: [Analysis] Main activities * Perform Measurement System Analysis (MSA) for analytical methods as deemed necessary. Expected results: Analytical methods deemed robust, rugged and statistically acceptable for use as intended Area of responsibility 6: [Routinely provide advice and assistance to team members regarding unique problems.] Main activities * Independently plan and execute analytical studies that may not be well defined, have multiple variables, and require advanced knowledge in analytical technique and principle * Proficiently perform Analytical Research Chemist I and II duties as assigned Expected results: Well-integrated new employee capable of performing job duties Profile Requirements (Diploma and experience) * BS Chemistry or equivalent science degrees with 5-10 years experience. Master's Degree preferred * 5+ years prior experience working in an analytical test lab with experience developing and validating methods Skills * This individual has previously demonstrated proficiency as an Analytical Chemist II and Analytical Project management, either within Virbac or at a previous employer Virbac provides numerous career opportunities, thanks to the diversity of its jobs and their international dimension. Joining Virbac means joining dynamic teams ambitious for success. Add Your Talent to Ours!

The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, apply with us today! Job Description Job Responsibilities and Requirements: The position will be providing analytical support to biotherapeutic process development teams, specifically focusing on large molecules (proteins, polysaccharides, nucleic acids, etc.). Candidates should have familiarity with several of the below laboratory techniques; they should also possess expertise/knowledge with: · Agarose Gel electrophoresis (AGE) · Capillary gel electrophoresis (CGE) · Quantitative polymerase chain reaction (qPCR) · Enzyme linked Immunosorbent Assay (ELISA) · Ultraviolet and visual light spectroscopy (UV-Vis) · Analytical chromatographic separations using HPLCs or UPLCs · Use of automated liquid handler Qualifications Experience with Capillary Gel Electrophoresis, qPCR and HPLC is required. Sec-MALS experience Bachelors or Masters Degree in Biotechnology, Biochemical Engineering, Analytical Chemistry, Chemical Engineering or other related fields. 3-5 years of relevant industrial experience Preferred experience: · Electronic laboratory notebook systems and/or GMP documentation practice · Empower or OpenLabs Software Additional Information Position is full-time, Monday to Friday 8:00AM - 4:00PM or 9:00AM - 5:00PM. Candidates currently living within a commutable distance of Chesterfield, MO are encouraged to apply. What we offer: · Comprehensive medical coverage, with dental and vision options · Life and disability insurance · Paid holidays and vacation. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

MilliporeSigma is building a new Novel Modalities R&D department to support cutting edge APIs in the pharma industry. With this new team, we will develop and provide the manufacturing platform for life saving drugs. Your role: We are hiring a Senior Analytical Scientist for our newly created Novel Modalities R&D organization. Reporting to the Head of Novel Modalities R&D, the Senior Analytical Scientist will develop and implement analytical methods for bioconjugates or RNA liposomes. Responsibilities: Lead the development efforts to deliver project milestones on-time and on-quality Understand challenges in the contract manufacturing industry and work to ensure MilliporeSigma is on the cutting edge of bioconjugation and liposomes Identify optimized solutions considering newest scientific data sources and interact with the scientific community in the areas of interest. Keep updated on product and industry knowledge and “best-in-class” analytical technologies Demonstrate attention to detail in the planning, execution and documentation of experimental work Drive implementation of digital tools and solutions in the development and manufacturing disciplines. Establish a team-based approach with other internal organizations, such as marketing, sales, PAD, QC and operations Drive innovation for R&D activities securing IP for internal MilliporeSigma technology and product platforms whenever suitable Establish relationships in the industry that provide access to direct customer feedback and creates opportunities for world-class responsiveness and innovative growth Deliver timely and comprehensive written and oral communications to both internal and external stakeholders Who You Are: Minimum Qualification: Bachelor's degree in Chemistry, Chemical Engineering, Biochemistry, Biology or other related Scientific discipline with 5+ years laboratory experience 3+ years of R&D experience 3+ years' experience in analytical techniques for bioconjugates or liposomes 3+ years' experience with HPLC, GC and /or particle characterization instruments Preferred Qualifications: PhD with 3+ years or Master's degree with 5+ years of ADC or liposomes industry experience Experience in CMO or CRO Working experience in cGMP/GLP, knowledgeable about ICH and FDA guidelines Experience with gene therapeutic is a plus Proficient in the modern pharmaceutical R&D and innovative analytical methods for bioconjugates and/or liposomes. Knowledge of analytical techniques in molecular biology is a plus. Proven ability to lead a team in technical excellence, project completion and people development Hands on experience in analytical method development and method transfer Desire to translate new science into new technologies and the ambition to succeed in an innovation driven environment PAT and Automation (medium to high-throughput) experience in analytical is highly desirable Excellent interpersonal skills and ability to work in global and multicultural environment Ability to train employees Excellent written and verbal communication skills Working knowledge of Microsoft Office, as well as experience with advanced data analysis and/or statistical software systems

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description The qualified candidate will be responsible for developing and implementing methods of analysis for characterization of proteins, peptides, vaccines, carbohydrates, and oligonucleotides using advanced analytical techniques. Qualifications • B.S. in chemistry, biochemistry, and biology, or equivalent; industrial experience in analytical characterization is desirable. • The qualified colleague must have knowledge in protein biochemistry and/or protein analytics. • Good communication and writing skills are essential due to the highly matrixed, fast-paced, project-team environment. Additional Information Thanks Warm Regards Ricky Bansal 732-429-1925

Job Details Laboratory - St Louis, MO 4 Year Degree $22.00 - $22.00 Hourly None DayNight Shift Analytical Chemist Our mission at Averhealth is to reclaim lives, unite families, and strengthen communities by creating and providing the smartest, most innovative solutions for substance use disorder monitoring and recovery. This is an excellent Entry-Level opportunity for recent grads in Chemistry, Biology, or Biochemistry! We are in need of a determined Analytical Chemists to join our St. Louis Laboratory Team. In this role, you will prepare specimens for routine drug testing following the laboratory's Standard Operating Procedures. The Analytical Chemist will also interface with our instruments (LC/MS/MS and GC/MS) and needs the ability to work safely with instruments/equipment, chemicals, and biological samples. PAY: $22/HR + Company-Paid Training Program + Attendance Bonus Eligibility + Uniform Allowance (post-training) + Referral Bonus Eligibility + Competitive Full-Time Benefits HOURS: Full-Time (40+ hours/week) SHIFTS AVAILABLE Monday - Friday (Nightshift) 9:00 PM - 5:30 AM Sunday - Thursday (Nightshift) 6:00PM - 2:30 AM ESSENTIAL DUTIES AND RESPONSIBILITIES Locate specific patient samples and perform confirmation assays according to the toxicology testing method requested. Communicate and interact with other departments to solve issues impeding confirmation tests on patient samples Interface with analytical instruments including LC-MS, GC-MS, and Tecan Liquid Handler. Review data generated by LC-MS and GC-MS instrumentation before sending it to data certifiers. Assist with training new staff on sample preparation, LC-MS/GC-MS operation, and data review. Lab maintenance: including, but not limited to, cleaning glassware, restocking/refilling pipette tips, glass vials, centrifuge tubes, etc. Reagent preparation Adhere to all security procedures for ensuring the confidentiality of donor information Adhere to all established guidelines outlined in Averhealth Employee Guidebook Other duties as assigned by the supervisor REQUIREMENTS Bachelor's Degree in Science or equivalent relevant field REQUIRED 1-3+ years experience operating and reviewing data for an LC-MS/MS instrument. ABSciex experience preferred. 1-3+ years experience in a biological laboratory environment. Experience with BOTH LC/MS/MS and/or GC/MS is an added advantage. COMPENSATION AND BENEFITS Pay Dependent on past qualifications and experience We offer Full-Time employees (working over 30 hours per week): Medical, Dental, Vision, Short Term Disability, Long Term Disability and Life Insurance with an employer contribution 3 weeks of Paid Time Off in your first year We offer ALL employees: Company-Paid Training Program Attendance Bonuses Annual Uniform Reimbursement (scrubs) 401k with an employer match Annual Raises Referral Bonuses Instant access to earned wages-no need to wait for your paycheck! Averhealth is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Averhealth is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Averhealth are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Averhealth will not tolerate discrimination or harassment based on any of these characteristics. Physical and Sensory Requirements: Mobility, walking, climbing, sitting, standing, reaching, bending, lifting (minimum of 10 lbs), carrying, pushing, pulling, fine eye-hand coordination, ability to read, write, listen and speak clearly, the ability to understand and follow written and oral instructions and directions, ability to drive a vehicle and travel, and ability to remain calm under pressure. Must be able to sit and/or stand for extended periods of time. Must be able to use computer, monitor, cell phone, mouse and keyboard extensively as well as other general office equipment.

Job Details Education Level: 4 Year Degree Salary Range: $22.00 - $22.00 Hourly Travel Percentage: None Job Shift: Day Night Shift Analytical Chemist Our mission at Averhealth is to reclaim lives, unite families, and strengthen communities by creating and providing the smartest, most innovative solutions for substance use disorder monitoring and recovery. This is an excellent Entry-Level opportunity for recent grads in Chemistry, Biology, or Biochemistry! We are in need of a determined Analytical Chemists to join our St. Louis Laboratory Team. In this role, you will prepare specimens for routine drug testing following the laboratory's Standard Operating Procedures. The Analytical Chemist will also interface with our instruments (LC/MS/MS and GC/MS) and needs the ability to work safely with instruments/equipment, chemicals, and biological samples. * PAY: $22/HR + Company-Paid Training Program + Attendance Bonus Eligibility + Uniform Allowance (post-training) + Referral Bonus Eligibility + Competitive Full-Time Benefits * HOURS: Full-Time (40+ hours/week) SHIFTS AVAILABLE Monday - Friday (Nightshift) 9:00 PM - 5:30 AM Sunday - Thursday (Nightshift) 6:00PM - 2:30 AM ESSENTIAL DUTIES AND RESPONSIBILITIES * Locate specific patient samples and perform confirmation assays according to the toxicology testing method requested. * Communicate and interact with other departments to solve issues impeding confirmation tests on patient samples * Interface with analytical instruments including LC-MS, GC-MS, and Tecan Liquid Handler. * Review data generated by LC-MS and GC-MS instrumentation before sending it to data certifiers. * Assist with training new staff on sample preparation, LC-MS/GC-MS operation, and data review. * Lab maintenance: including, but not limited to, cleaning glassware, restocking/refilling pipette tips, glass vials, centrifuge tubes, etc. * Reagent preparation * Adhere to all security procedures for ensuring the confidentiality of donor information * Adhere to all established guidelines outlined in Averhealth Employee Guidebook * Other duties as assigned by the supervisor REQUIREMENTS * Bachelor's Degree in Science or equivalent relevant field REQUIRED * 1-3+ years experience operating and reviewing data for an LC-MS/MS instrument. ABSciex experience preferred. * 1-3+ years experience in a biological laboratory environment. * Experience with BOTH LC/MS/MS and/or GC/MS is an added advantage. COMPENSATION AND BENEFITS * Pay Dependent on past qualifications and experience * We offer Full-Time employees (working over 30 hours per week): * Medical, Dental, Vision, Short Term Disability, Long Term Disability and Life Insurance with an employer contribution * 3 weeks of Paid Time Off in your first year * We offer ALL employees: * Company-Paid Training Program * Attendance Bonuses * Annual Uniform Reimbursement (scrubs) * 401k with an employer match * Annual Raises * Referral Bonuses * Instant access to earned wages-no need to wait for your paycheck! Averhealth is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Averhealth is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Averhealth are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Averhealth will not tolerate discrimination or harassment based on any of these characteristics. Physical and Sensory Requirements: Mobility, walking, climbing, sitting, standing, reaching, bending, lifting (minimum of 10 lbs), carrying, pushing, pulling, fine eye-hand coordination, ability to read, write, listen and speak clearly, the ability to understand and follow written and oral instructions and directions, ability to drive a vehicle and travel, and ability to remain calm under pressure. Must be able to sit and/or stand for extended periods of time. Must be able to use computer, monitor, cell phone, mouse and keyboard extensively as well as other general office equipment. Our mission at Averhealth is to reclaim lives, unite families, and strengthen communities by creating and providing the smartest, most innovative solutions for substance use disorder monitoring and recovery. This is an excellent Entry-Level opportunity for recent grads in Chemistry, Biology, or Biochemistry! We are in need of a determined Analytical Chemists to join our St. Louis Laboratory Team. In this role, you will prepare specimens for routine drug testing following the laboratory's Standard Operating Procedures. The Analytical Chemist will also interface with our instruments (LC/MS/MS and GC/MS) and needs the ability to work safely with instruments/equipment, chemicals, and biological samples. * PAY: $22/HR + Company-Paid Training Program + Attendance Bonus Eligibility + Uniform Allowance (post-training) + Referral Bonus Eligibility + Competitive Full-Time Benefits * HOURS: Full-Time (40+ hours/week) SHIFTS AVAILABLE Monday - Friday (Nightshift) 9:00 PM - 5:30 AM Sunday - Thursday (Nightshift) 6:00PM - 2:30 AM ESSENTIAL DUTIES AND RESPONSIBILITIES * Locate specific patient samples and perform confirmation assays according to the toxicology testing method requested. * Communicate and interact with other departments to solve issues impeding confirmation tests on patient samples * Interface with analytical instruments including LC-MS, GC-MS, and Tecan Liquid Handler. * Review data generated by LC-MS and GC-MS instrumentation before sending it to data certifiers. * Assist with training new staff on sample preparation, LC-MS/GC-MS operation, and data review. * Lab maintenance: including, but not limited to, cleaning glassware, restocking/refilling pipette tips, glass vials, centrifuge tubes, etc. * Reagent preparation * Adhere to all security procedures for ensuring the confidentiality of donor information * Adhere to all established guidelines outlined in Averhealth Employee Guidebook * Other duties as assigned by the supervisor REQUIREMENTS * Bachelor's Degree in Science or equivalent relevant field REQUIRED * 1-3+ years experience operating and reviewing data for an LC-MS/MS instrument. ABSciex experience preferred. * 1-3+ years experience in a biological laboratory environment. * Experience with BOTH LC/MS/MS and/or GC/MS is an added advantage. COMPENSATION AND BENEFITS * Pay Dependent on past qualifications and experience * We offer Full-Time employees (working over 30 hours per week): * Medical, Dental, Vision, Short Term Disability, Long Term Disability and Life Insurance with an employer contribution * 3 weeks of Paid Time Off in your first year * We offer ALL employees: * Company-Paid Training Program * Attendance Bonuses * Annual Uniform Reimbursement (scrubs) * 401k with an employer match * Annual Raises * Referral Bonuses * Instant access to earned wages-no need to wait for your paycheck! Averhealth is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: Averhealth is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Averhealth are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. Averhealth will not tolerate discrimination or harassment based on any of these characteristics. Physical and Sensory Requirements: Mobility, walking, climbing, sitting, standing, reaching, bending, lifting (minimum of 10 lbs), carrying, pushing, pulling, fine eye-hand coordination, ability to read, write, listen and speak clearly, the ability to understand and follow written and oral instructions and directions, ability to drive a vehicle and travel, and ability to remain calm under pressure. Must be able to sit and/or stand for extended periods of time. Must be able to use computer, monitor, cell phone, mouse and keyboard extensively as well as other general office equipment.

At the dawn of the new millennium, a unique information technology company was born: HCL Technologies. As narrated in the video below, HCL Technologies has demonstrated remarkable growth through the recent economic downturn, emerging as one of only eight 21st century listed technology companies in the world to cross $1bn in Net Profit, $6bn in Revenue and $15bn in Market Capitalization. Job Description • Molecular biologist to aid in characterization of recombinant mammalian cell lines. Requires BS/MS in molecular biology or related field and at least one year of laboratory experience. • Must be familiar with general cell culture techniques (ex. aseptic passaging of cell lines), RNA, cDNA and genomic DNA preparation, DNA/RNA electrophoresis, and Northern and Southern analyses. • Experience with molecular cloning techniques such as plasmid construction, preparation and analysis, DNA sequencing technologies and analysis of DNA sequencing data multiple sequence alignments, identification of mutant sequences, in silico protein translation, etc. would be a definite plus MOST CRITICAL SKILLS: gDNA/RNA preparation; northern/southern blot analysis. Additional Skills:REQUIRED PERSONALITY TRAITS: team oriented, fast learner, good attention. MOST CRITICAL SKILLS: gDNA/RNA preparation; northern/southern blot analysis. Additional Information Best Regards, Anuj Mehta ************

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: As the Associate Production Scientist with MilliporeSigma, your role is to support our Small Molecule Bio-Organic product lines. You will work with other production scientists and operators, and SMEs to ensure successful manufacturing of an established line of products and troubleshoot and investigate process issues that arise. You will write and modify procedures consistent with quality guidelines and identify potential process improvements while interacting cross-functionally with Quality Control, Quality Assurance, Packaging, Materials Management, Engineering and Maintenance. * Day Shift- Monday-Friday 8am-4pm * Safely perform operations to meet quality expectations. * Perform multi-disciplined, established processes, assays and/or unit operations, primarily those requiring a higher level of skill and knowledge. * Contribute to support functions of the lab (e.g., maintain equipment, prepare reagents, restock lab supplies, waste disposal). * Clean-up equipment and working areas during and after operations. * Communicate the status of operations and bring deviations to the attention of supervisor. * Ensure all applicable logbooks have been filled out completely as required by current procedures. * Participate as needed in quality audits. * Accurately perform in-process testing and assays. * Identify problems and limitations of analysis. * Perform routine troubleshooting. * In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles. * Participate in process improvements under the guidance of a Supervisor or Scientist. * Take the necessary action to resolve any unsafe conditions. * Perform and interpret analytical evaluations of products and intermediates. Physical Attributes: * Wearing of personal protective equipment such as respirator or chemical protective clothing for extended periods. * Lifting and pushing up to 50 pounds. Who You Are Minimum Qualifications: * Bachelor's Degree in Chemistry, Biochemistry, Biology, or related life science discipline. Preferred Qualifications: * Knowledge in chemistry or biochemistry, math, and general science. * Familiar with laboratory instruments and production equipment. * Analytical techniques and equipment. * Safe chemical handling methods experience. * Good communication skills, verbal and written. * Mechanical skills. * Troubleshooting skills. * Interpersonal skills. * Organizational skills. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team! If you would like to know more about what diversity, equity, and inclusion means to us, please visit ********************************************************

We make pet food taste great! For over 30 years, AFB International has been providing pet food solutions that enrich the lives of pets and their people. Our palatants are specially designed to make pet foods, treats and supplements taste better, ensuring pets receive the vital nutrients they need. We know wagging tails, licking whiskers and empty bowls equal happy pets and happy pet parents. Join AFB and you'll be a part of a team of highly skilled professionals that provide the greatest contribution to our success as an organization. Our team members are diverse, creative, passionate experts who are genuinely dedicated to our mission, our customers, and the pets we serve worldwide. Job Description Your opportunity within AFB International As our Science & Technology Product Development Scientist (level will be based on experience and education), you will play a critical in the global Research & Development driving product sciences to deliver successful new products, scale-up of new technology, taking supply assurance of raw materials into consideration, management of critical risk factors in product development and provide technical support to operations. The main responsibility in this role is to develop new palatants meeting the criteria of internal and external stakeholders and strengthen our product portfolio. In this role, you will report to the Global Head of Product Sciences. Key Responsibilities • Technical lead for the development of key new products to enable the Science & Technology pipeline strategy with a focus on dry dog and cat palatants. • Lead multi-disciplinary teams responsible for innovation projects from concept to execution. • Leverage deep expertise in raw material knowledge, particularly in areas such as yeast, to develop robust chassis models for new product development. • Conduct lab work to develop new dry products and to evaluate new products with analytical capabilities (e.g. NIR, colorimeter). • Optimize and improve existing technologies to provide new product capability, higher product quality, or improve manufacturing efficiency. • Collaborate with external partners such as suppliers, research institutions, and academic experts to leverage external knowledge and capabilities in product development. • Develop and execute the trial plan and risk management process for new product development and implementation. • Work closely with Regulatory Affairs to ensure compliance with relevant regulations and standards throughout the product development process. • Lead pilot plant spray drying activities and utilize expertise, like glass transition to optimize drying conditions and product stability. • Partner with Process Sciences and manage critical processing risks to ensure a seamless implementation from new product concept to production. • Utilize expertise in dry processing techniques (blending and drying) and equipment to upscale recipes from laboratory to factory, ensuring product quality, stability, and consistency. Collaborate with Process Sciences and Engineering teams for seamless implementation. • Provide product support to the Manufacturing sites through an intimate technical knowledge of processproduct interactions. • Perform data analysis on the generated data in experimental designs and analytical trials. • Responsible for communication (both written and verbal) of key project / technical findings (presentations and technical reports), informs project team and key stakeholders for further decision making. Education & Professional Qualification • BSc/MSc in Food/Chemical - Engineering, Technology or Science discipline. • Minimum 2 years' experience with the ability to demonstrate a proven track record in food related technologies. Experience should include product development and scale-up. Knowledge/Experience • Good understanding of food technology, chemistry, microbiology, food assurance and sensory science through academic and practical experiences. • Experience in formulating recipes. • Experience in spray drying technology, familiar with things like glass transition. • Experienced in using research methods, experimental designs, and data analysis, • Understand fundamentals of good project management and be able to use in the projects on daily basis. • Excellent (Dutch and) English verbal and written communication skills. • Basic understanding of food manufacturing practices and quality standards. Competencies • Accurate and strong analytical skills. • Hands on mentality, able to work in a lab/pilot environment to create products. • Result and data driven oriented combined with entrepreneurial and innovative mindset. • Excellent communication and presentation skills. • Good sense of teamwork and proactive networking skills. • Ability to prioritize and oversee multiple projects in a fast-paced environment. • Strong interpersonal skills and able to collaborate with cross-functional teams including procurement, sales and operations. AFB International is an Equal Opportunity Employer (EOE). Qualified applicants are considered for employment without regard to race, religion, color, sex, age, disability, sexual orientation, genetic information, national origin, or veteran status.

Opportunity to work for a team that collaborates, open to new ideas that improves efficiency and has cross training opportunities. You and Your Job As a Quality Control Analyst you will be successful at identifying deficiencies to improve the current process. The Financial Crime Compliance is a part of Compliance, Rabo Diversified Services (RDS). This group provides compliance advisory and support services to the NY Branch, RSI, Canada Branch, Mexico Representative Office, Utrecht America Holdings and Rabo AgriFinance. The FCC Quality Control (QC) /Monitoring Analyst will execute ongoing QC/monitoring assessments based on established Key Risk Indicators (KRIs) for various compliance related internal controls pertaining to (but not limited to) Client due diligence, Transaction Monitoring, Suspicious Activity Reporting, 314(a), 314(b), OFAC/Sanctions & Watchlist Screening, CIP, and Section 311 & 9714 Special Measures. The QC/monitoring function is an important governance and oversight component which aids in the continuing evaluation of control effectiveness and potential deficiencies related to the BSA AML Compliance & OFAC Program Job Responsibilities Provide ongoing support by thorough execution of QC assessments which aid in ensuring adherence to laws and regulations relevant to BSA AML Compliance & OFAC/Sanctions. Provide updates on the QC/monitoring results to the BSA AML Compliance & OFAC QC Manager on a regular basis, in accordance with established processes. Contribute to the development and maintenance of QC policies, procedures, and compliance tools. Continuously maintain and expand knowledge pertaining to AML/CFT, BSA, OFAC/Sanctions compliance related regulations and industry practices. Act on own initiative where appropriate to meet business objectives, while remaining in line with established policies and procedures. Assist in coaching, training, and developing other BSA AML Compliance & OFAC QC Analysts. Raise risks/gaps identified to the BSA AML Compliance & OFAC QC Manager and propose solutions. Assist with the development and implementation of QC processes as applicable. Your Promise to Us: To be considered for the Quality Control Analyst role, you must have: Bachelor's degree 2+ years' experience in Financial crime compliance. Legally authorized to work in the United States on a full-time basis. Rabobank is unable to sponsor or take over sponsorship of an employment visa for this position. Our Commitment to you - cultivating your way beyond pay: Rabobank embraces diversity and welcomes employees and applicants of all backgrounds. Our goal is to always create an environment that is inclusive, drawing upon the strengths of the diversity of our workforce to exceed the expectations of our clients and customers. We view your well-being as much more than a paycheck. We continually evaluate and evolve our benefit offerings to be comprehensive, competitive and to give you the options and the flexibility you need. We focus our employee benefits on three main components: Physical Well-Being includes our commitment to your Health and Wellness. Medical, Dental and Vision plan coverages are effective on your date of hire. Rabo offers multiple plan options and a full network of providers to best meet your needs. Financial Well-Being provides for your Retirement + Savings + Security. We love seeing your retirement plan balance grow just as much as you do! That's why you can start participating in the 401(k) plan on your date of hire. Plus we match 50% of the first 6% you contribute to your 401(k) plan for US Employees. Rabo also contributes an additional 3% of your eligible pay in Safe Harbor contribution and up to 3% in annual Discretionary Profit Sharing contributions. Emotional Well-Being ensures your Work + Life balance. We offer a generous paid time off program to full time employees: up to 20 days of vacation time, 5 days of additional time off plus 7 sick days and 11 US holidays annually (based on hire date during the calendar year). In addition, Growing a Better World Together requires wanting the best for our employees and their families and our communities. To do that, we offer both the time and financial support to give back to the community through our Dollars for Doers, Helping Hands and Gift Matching programs. (All paid time off is subject to company accrual and carryover policies.) Our Organization: Rabobank Group is a global financial services leader providing wholesale and retail banking, leasing, and real estate services in more than 37 countries worldwide. Founded over a century ago, Rabobank today is one of the world's largest banks with over $678 billion in assets. In North America, Rabobank is a premier corporate and investment bank to the food, agribusiness, commodities and energy industries in the United States, Mexico, and Canada. Rabo AgriFinance, a subsidiary of Rabobank, is a leading financial services provider for farmers, ranchers and agribusinesses in the United States and Canada. Together, we provide sector expertise, strategic counsel and tailored financial solutions to clients across the entire value chain. Visit ****************** Salary Expectations: Target Hiring Range Saint Louis, MO: $70,000.00 - $83,000.00 Target Hiring Range New York, NY: $80,000.00 - $93,000.00 This position is subject to the terms of [RAF/Rabobank/RDS]'s compensation plans and policies. It is anticipated that the position will pay within the target hiring range. The range is reflective of the desired primary physical work location and may be adjusted outside of the projected range based on geographical differentiation if the actual work location of the hired candidate differs from the desired primary location, or for other lawful reasons. Further, all full-time regular positions include all other benefits provided to [RAF/Rabobank/RDS] employees, including healthcare benefits, 401k matching, vacation, sick leave, parental leave, possible discretionary bonuses and all other benefits that are all governed by and subject to ERISA plan documents and eligibility. Rabo provides equal opportunity in employment to all employees and applicants and does not discriminate on the basis of race, color, creed, religion, national origin, ancestry, alienage or citizenship status, age, sex, sexual orientation, gender identity gender expression, marital status, genetic information, medical condition, physical or mental disability, pregnancy, childbirth or related medical condition, military service or veteran status, victims of domestic violence, or any other basis protected by applicable law. Rabo also prohibits harassment of any individuals on any of the bases listed above. At Rabobank, we strive to grow a better world together. In order to achieve that, we have to have the right people in the right jobs. Are you ready to join our team? This job posting has no fixed application deadline. We will accept resumes until a qualified applicant pool is identified. #LI-Hybrid